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Dynamics of the excised base release in thymine DNA glycosylase during DNA repair process

机译:DNA修复过程中胸腺嘧啶DNA糖基化酶中被切除的碱基释放的动力学

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摘要

Thymine DNA glycosylase (TDG) initiates base excision repair by cleaving the N-glycosidic bond between the sugar and target base. After catalysis, the release of excised base is a requisite step to terminate the catalytic cycle and liberate the TDG for the following enzymatic reactions. However, an atomistic-level understanding of the dynamics of the product release process in TDG remains unknown. Here, by employing molecular dynamics simulations combined with the Markov State Model, we reveal the dynamics of the thymine release after the excision at microseconds timescale and all-atom resolution. We identify several key metastable states of the thymine and its dominant releasing pathway. Notably, after replacing the TDG residue Gly142 with tyrosine, the thymine release is delayed compared to the wild-type (wt) TDG, as supported by our potential of mean force (PMF) calculations. These findings warrant further experimental tests to potentially trap the excised base in the active site of TDG after the catalysis, which had been unsuccessful by previous attempts. Finally, we extended our studies to other TDG products, including the uracil, 5hmU, 5fC and 5caC bases in order to compare the product release for different targeting bases in the TDG–DNA complex.
机译:胸腺嘧啶DNA糖基化酶(TDG)通过切割糖和靶标碱基之间的N-糖苷键来启动碱基切除修复。催化后,释放离去的碱是终止催化循环和释放TDG的必要步骤,以用于后续的酶促反应。但是,对于TDG中的产品发布过程的动力学,尚无原子级的了解。在这里,通过结合分子动力学模拟和马尔可夫状态模型,我们揭示了在微秒时标和全原子分辨率下,胸腺嘧啶释放后的动力学。我们确定了胸腺嘧啶及其主要的释放途径的几个关键的亚稳态。值得注意的是,在将TDG残基Gly142替换为酪氨酸后,与野生型(wt)TDG相比,胸腺嘧啶的释放被延迟了,这受到我们平均力(PMF)计算潜力的支持。这些发现需要进行进一步的实验测试,以将被切除的碱基潜在地捕获在催化后的TDG活性位点中,而先​​前的尝试并未成功。最后,我们将研究扩展到其他TDG产品,包括尿嘧啶,5hmU,5fC和5caC碱基,以比较TDG-DNA复合物中不同靶向碱基的产品释放。

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